Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/31730
Title: Controlled synthesis and analysis of He-H<sup>+</sup> <inf>3</inf> in a 3.7 K ion trap
Authors: Savić Igor 
Gerlich Dieter
Asvany Oskar
Jusko Pavol
Schlemmer Stephan
Issue Date: 2015
Journal: Molecular Physics
Abstract: © 2015 Taylor & Francis. Complexes of the triatomic hydrogen ion with helium were synthesised in a low-temperature 22-pole rf ion trap at He number densities of up to 10<sup>16</sup> cm<sup>-</sup><sup>3</sup>. Absolute ternary rate coefficients for sequentially attaching He atoms have been determined from the growth of complexes with increasing storage time. The number of helium-tagged ions is significantly reduced when increasing the nominal temperature from 4 to 25 K. Competition between attachment and dissociation via collisions leads to stationary H<inf>e</inf><inf>n</inf>-H<sup>+</sup><inf>3</inf> (n up to 9) distributions. State-specific excitation of the trapped H<sup>+</sup><inf>3</inf> ions via IR transitions significantly reduces the formation of complexes. Tuning the laser to Δv<inf>2</inf> = 1 transitions in the range of 2726 cm<sup>-</sup><sup>1</sup> leads to LIICG lines, i.e., to spectra caused by laser-induced inhibition of complex growth. In addition, almost 100 lines have been found between 2700 and 2765 cm<sup>-</sup><sup>1</sup>, which are attributed to laser-induced dissociation of the in situ formed He-H<sup>+</sup><inf>3</inf> complex ions. These lines are not yet assigned; however, their absorption strength, statistics and predissociation lifetimes provide interesting information on both the stable complexes as well as on scattering resonances in low-energy H<sup>+</sup><inf>3</inf>+He collisions. New calculations of the potential energy surface will help to analyse the dissociation spectrum. There are some indications that para-H<sup>+</sup><inf>3</inf> is enriched under the conditions of the present experiment.
URI: https://open.uns.ac.rs/handle/123456789/31730
ISSN: 0026-8976
DOI: 10.1080/00268976.2015.1037802
Appears in Collections:PMF Publikacije/Publications

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